Canonical Allele Identifier: CA233603724

Gene: GYS2

Linked Data

• dbSNP Id: rs1008743783
• gnomAD v3: 12-21559413-T-G
• gnomAD v4: 12-21559413-T-G
• MyVariant Identifiers: chr12:g.21712347T>G (hg19) ; chr12:g.21559413T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21559413T>G , CM000674.2:g.21559413T>G	GRCh38
NC_000012.11:g.21712347T>G , CM000674.1:g.21712347T>G	GRCh37
NC_000012.10:g.21603614T>G	NCBI36
NG_016167.1:g.50435A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.1229+238A>C MANE Select	ENSP00000261195.2:n.1229+238A>C
ENST00000647960.1:c.*1231+238A>C	ENSP00000497202.1:n.*1231+238A>C
ENST00000648372.1:n.1156+238A>C
ENST00000261195.2:c.1229+238A>C	ENSP00000261195.2:n.1229+238A>C
NM_021957.3:c.1229+238A>C	NP_068776.2:n.1229+238A>C
XM_005253352.1:c.1229+238A>C	XP_005253409.1:n.1229+238A>C
XM_005253354.2:c.1010+238A>C	XP_005253411.1:n.1010+238A>C
XM_006719062.2:c.1229+238A>C	XP_006719125.1:n.1229+238A>C
XM_006719063.2:c.998+238A>C	XP_006719126.1:n.998+238A>C
NM_021957.4:c.1229+238A>C MANE Select	NP_068776.2:n.1229+238A>C
XM_006719063.3:c.998+238A>C	XP_006719126.1:n.998+238A>C
XM_024448960.1:c.1229+238A>C	XP_024304728.1:n.1229+238A>C